22380-94-5 Usage
Uses
Used in Organic Synthesis:
2,2-diMethylnaphtho[1,8-de][1,3]dioxine is utilized as a key intermediate in the synthesis of a variety of organic compounds. Its unique structure allows for the creation of complex molecules that can be used in different chemical reactions, contributing to the development of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-diMethylnaphtho[1,8-de][1,3]dioxine is employed as a building block for the development of novel drug candidates. Its distinctive chemical properties make it a valuable component in the design of new pharmaceuticals, potentially leading to the discovery of innovative treatments for various diseases.
Used in Molecular Materials:
2,2-diMethylnaphtho[1,8-de][1,3]dioxine is also used as a component in the development of molecular materials. Its unique structure and properties can contribute to the creation of advanced materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be applied in various fields, including electronics, energy, and environmental technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 22380-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,8 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22380-94:
(7*2)+(6*2)+(5*3)+(4*8)+(3*0)+(2*9)+(1*4)=95
95 % 10 = 5
So 22380-94-5 is a valid CAS Registry Number.
22380-94-5Relevant academic research and scientific papers
Murphy, Annabel C.,Devenish, Sean R. A.,Muscroft-Taylor, Andrew C.,Blunt, John W.,Munro, Murray H. G.
, p. 3854 - 3862 (2008)
An exploration of the chemistry of the spiro-mamakone system, exemplified by the cytotoxic, fungal metabolite spiro-mamakone A, is presented. The first reported synthesis of the spiro-mamakone carbon skeleton was achieved, as well as the synthesis of a variety of closely related analogues of the natural product. Biological testing of the synthetic analogues generated a structure-activity profile for the natural product, establishing the importance of the enedione moiety to biological activity. The Royal Society of Chemistry 2008.
